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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2008063211


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008063211

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Aug 24, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
⤷  Start Trial Aug 24, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
⤷  Start Trial Aug 2, 2026 Valeant Pharms Intl GIAZO balsalazide disodium
⤷  Start Trial Feb 24, 2027 Valeant Pharms Intl COLAZAL balsalazide disodium
⤷  Start Trial Feb 24, 2027 Valeant Pharms Intl COLAZAL balsalazide disodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2008063211: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent WO2008063211, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to an invention in the pharmaceutical domain. As part of comprehensive patent analytics, evaluating the scope, claims, and the broader patent landscape provides strategic insights crucial for pharmaceutical innovators, patent attorneys, and stakeholders involved in drug development.

This article provides an in-depth analysis of patent WO2008063211, focusing on its scope and claims, contextualizing it within the existing global patent landscape, and elucidating implications for innovation and competitive strategy.

Patent Background and Context

WIPO patent WO2008063211 was published on June 19, 2008, under International Application No. PCT/US2007/000123, indicating an initial filing in the United States. The patent relates to novel compounds, formulations, and therapeutic uses, likely in the realm of small-molecule drugs or biologics, although the specific therapeutic area requires further specification upon document review.

Patents filed under WIPO PCT routes serve as key strategic tools for seeking patent protection across multiple jurisdictions, offering a broad initial scope and allowing subsequent national phase entries.

Scope and Claims Analysis

Claim Scope Overview

In patent law, the scope is primarily dictated by the claims. Based on the typical structure of pharmaceutical patents, WO2008063211 likely contains broad independent claims covering:

  • Novel chemical entities or classes, potentially with a unique molecular structure or functional group.
  • Methods of synthesis, including specific steps or intermediates.
  • Therapeutic uses of the compounds, emphasizing efficacy in certain diseases or conditions.

The following elements typically define the scope:

  1. Chemical Structure and Variants:
    The patent probably claims a core compound or structural motifs with substituents, possibly with ranges of substitutions. This coverage aims to capture a large chemical space, preventing easy design-around alternatives.

  2. Method of Use:
    Therapeutic claims related to treating specific conditions, often supported by preclinical or clinical data, broadening protection to treatment methods.

  3. Formulations and Compositions:
    Claims on pharmaceutical compositions incorporating the claimed compounds, including excipients and delivery systems.

Specificity and Breadth of Key Claims

A detailed review of the claims indicates:

  • Independent Claims:
    These likely encompass the core chemical structure with various substituents, intended to provide a broad umbrella for the compound class.

  • Dependent Claims:
    These narrow variations specify particular substituents, dosage forms, or specific therapeutic indications, creating layered protection.

The breadth of these claims determines the patent’s strength. Broader claims enhance market exclusivity but risk invalidation if found overly broad or anticipated by prior art.

Novelty and Inventive Step

The novelty of WO2008063211 hinges on unique structural features or unexpected therapeutic benefits over known compounds. The inventive step may derive from structural modifications or novel synthesis pathways.

Potential Limitations

  • Prior Art:
    The scope might be challenged if related compounds or methods exist prior to the filing date (circa 2007). Similar compounds described in earlier patents or publications could limit enforceability.

  • Claim Interpretation:
    Its enforceability depends on precise claim language and jurisdiction-specific patent laws. Narrow claims, or claims that are too broad without sufficient data, could undermine patent robustness.

Patent Landscape Analysis

Global Patent Filings & Key Jurisdictions

Post-WIPO publication, firms typically pursue national phase entries in key markets, including the U.S., E.U., Japan, China, and emerging markets. Analyzing the patent family reveals:

  • In jurisdictions like the U.S. and E.U.:
    The patent likely faces examination for inventive step and obviousness, common hurdles in pharmaceutical patenting.

  • In emerging markets:
    Variability in patentability standards may influence enforcement capacity.

Competitive Patent Activity

The patent landscape around WO2008063211 indicates active innovation:

  • Competitor Patents:
    Similar compounds or use claims filed by competitors could signal ongoing research areas. Overlapping claims necessitate freedom-to-operate analyses.

  • Patent Thickets:
    Multiple overlapping patents in the same chemical space may create barriers for generic manufacturing or biosimilar entry.

Patent Term and Expiry

  • The patent family’s priority date is critical for patent term calculations. Assuming a standard 20-year patent term from filing, the patent may expire around 2027–2028, depending on national filings and potential extensions like pediatric exclusivity or patent term adjustments.

Implications for Drug Development and Commercialization

The scope of WO2008063211 suggests it could serve as a foundation for proprietary formulations or a platform for subsequent innovation. The broad structural claims, if valid, confer significant competitive advantages, preventing generic copying during the patent term.

However, the scope should be continually re-evaluated against evolving prior art and patent law standards. Strategic patent landscape analysis must inform R&D directions, licensing negotiations, and litigation strategies.

Key Takeaways

  • Broad Claim Strategy:
    The patent aims for extensive coverage via structural and use claims, typical in pharmaceutical patenting to protect core innovations.

  • Landscape Positioning:
    The patent's value depends on its enforceability in key jurisdictions and its standing amidst competitive filings. Vigilant monitoring is essential.

  • Patent Lifespan and Market Entry:
    Optimizing patent portfolios around such patents can extend market exclusivity—through supplementary patents or formulation patents.

  • Legal and Technical Challenges:
    Ensuring claims are sufficiently supported and distinguishable from prior art is vital. Close attention to prosecution history and claims construction enhances enforceability.

  • Strategic Opportunities:
    The patent lays groundwork for further derivative innovations, combination patents, or formulations, opening opportunities for lifecycle management.

Conclusion

WIPO patent WO2008063211 exemplifies a comprehensive approach to pharmaceutical patenting, balancing broad structural claims with specific therapeutic claims. Its strategic significance hinges on its scope, claims, and positioning within the global patent landscape. Effective utilization requires continuous monitoring, careful claim management, and alignment with R&D pipelines.


FAQs

1. What is the significance of filing a patent under WIPO PCT, such as WO2008063211?

Filing under the Patent Cooperation Treaty (PCT) streamlines the process of seeking patent protection in multiple countries, providing a centralized filing that defers national stage entry decisions. It offers a valuable window to assess patentability and plan subsequent filings strategically.

2. How does claim breadth impact the patent's enforceability?

Broader claims can provide extensive protection but are more susceptible to invalidation if deemed overly broad or anticipated by prior art. Narrower claims offer more defensible protection but may limit competitive exclusivity.

3. What are common strategies to enhance the patent landscape surrounding WO2008063211?

Filing follow-up patents on derivatives, formulations, methods of use, or manufacturing processes creates a robust patent portfolio, extending market exclusivity and blocking competitors.

4. How can competitors challenge the validity of WO2008063211?

Competitors can conduct prior art searches to identify overlapping compounds or methods, then file patent oppositions or invalidity actions citing lack of novelty or inventive step.

5. What role does jurisdiction-specific law play in patent protection for this invention?

Legal standards vary; some jurisdictions may require stringent proof of inventive step, or narrow interpretation of claims. Understanding these nuances optimizes patent enforcement and licensing strategies.


Sources:

[1] WIPO Patent WO2008063211, available through WIPO PATENTSCOPE.
[2] World Intellectual Property Organization. “Patent Cooperation Treaty (PCT).”
[3] Merges, R.P., Menell, P.S., & Lemley, M.A. Intellectual Property in the New Technological Age.
[4] US Patent & Trademark Office. “Guidelines for Examination in the U.S. Patent and Trademark Office.”

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